A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005092



Internal ID18747623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16876990..16920575hg38UCSC Ensembl
Innerchr1:17203485..17247070hg19UCSC Ensembl
Innerchr1:17076072..17119657hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3843586
hg1943586
hg1843586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv112n100
Supporting Variantsnssv3480171, nssv3466354, nssv3474718
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005092
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer