A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3698882



Internal ID18650477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16596505..16643671hg38UCSC Ensembl
Innerchr1:16923000..16970166hg19UCSC Ensembl
Innerchr1:16795587..16842753hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3847167
hg1947167
hg1847167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013386
Supporting Variants
Samples
Known GenesCROCCP2, NBPF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3698882
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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