A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043957



Internal ID19133176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20895177..20952929hg38UCSC Ensembl
Innerchr14:21363336..21421088hg19UCSC Ensembl
Innerchr14:20433176..20490928hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3857753
hg1957753
hg1857753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1802n100
Supporting Variantsnssv3532134, nssv3532159, nssv3532160, nssv3532149, nssv3532139, nssv3532150, nssv3532161, nssv3532133, nssv3532132, nssv3532141, nssv3532127, nssv3532156, nssv3532137, nssv3532138, nssv3532155, nssv3532128, nssv3532145, nssv3532130, nssv3532164, nssv3532157, nssv3532147, nssv3532136, nssv3532143, nssv3532162, nssv3532158, nssv3532154, nssv3532148, nssv3532140, nssv3532163, nssv3532153, nssv3532142, nssv3532131, nssv3532151, nssv3532125, nssv3532126, nssv3532152, nssv3532144, nssv3532135, nssv3532146, nssv3532129
Samples
Known GenesECRP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043957
Frequency
Sample Size11257
Observed Gain0
Observed Loss40
Observed Complex0
Frequencyn/a


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