A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997518



Internal ID18810368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16909177..16934111hg38UCSC Ensembl
Innerchr1:17235672..17260606hg19UCSC Ensembl
Innerchr1:17108259..17133193hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3824935
hg1924935
hg1824935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv123n100
Supporting Variantsnssv3466222, nssv3470163
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)nsv997518
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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