A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999057



Internal ID18811907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16890896..16931632hg38UCSC Ensembl
Innerchr1:17217391..17258127hg19UCSC Ensembl
Innerchr1:17089978..17130714hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3840737
hg1940737
hg1840737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv115n100
Supporting Variantsnssv3471303, nssv3475822
Samples
Known GenesCROCC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999057
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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