A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018638



Internal ID19107855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:51527881..51569575hg38UCSC Ensembl
Innerchr7:51595578..51637272hg19UCSC Ensembl
Innerchr7:51563072..51604766hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3841695
hg1941695
hg1841695
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6348n100
Supporting Variantsnssv3661269, nssv3661270
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)nsv1018638
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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