A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970815



Internal ID18606037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:35081519..35092614hg38UCSC Ensembl
Innerchr7:35121131..35132226hg19UCSC Ensembl
Innerchr7:35087656..35098751hg18UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3811096
hg1911096
hg1811096
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2442138, nssv2442135, nssv2442136, nssv2442137, nssv2442134, nssv2442140, nssv2442141, nssv2442132, nssv2442139, nssv2442133
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDPY19L2P1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970815
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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