A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021303



Internal ID18763837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88017440..88043065hg38UCSC Ensembl
Innerchr7:87646755..87672380hg19UCSC Ensembl
Innerchr7:87484691..87510316hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3825626
hg1925626
hg1825626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6523n100
Supporting Variantsnssv3755430, nssv3655191
Samples
Known GenesADAM22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021303
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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