A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034553



Internal ID19123775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:122094880..122160326hg38UCSC Ensembl
Innerchr7:121734934..121800380hg19UCSC Ensembl
Innerchr7:121522170..121587616hg18UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3865447
hg1965447
hg1865447
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6602n100
Supporting Variantsnssv3662115, nssv3662116, nssv3662114
Samples
Known GenesAASS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034553
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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