A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002908



Internal ID18745440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16876990..16931994hg38UCSC Ensembl
Innerchr1:17203485..17258489hg19UCSC Ensembl
Innerchr1:17076072..17131076hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3855005
hg1955005
hg1855005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv115n100
Supporting Variantsnssv3471540, nssv3464638
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)nsv1002908
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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