A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999431



Internal ID18812281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16876990..16931436hg38UCSC Ensembl
Innerchr1:17203485..17257931hg19UCSC Ensembl
Innerchr1:17076072..17130518hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3854447
hg1954447
hg1854447
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv115n100
Supporting Variantsnssv3464244, nssv3480252, nssv3466241, nssv3471754, nssv3471515, nssv3469727, nssv3475701, nssv3478587, nssv3479782, nssv3465258, nssv3482597, nssv3476461, nssv3479351, nssv3470139
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)nsv999431
Frequency
Sample Size29084
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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