A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969617



Internal ID19227229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:140176300..140177200hg38UCSC Ensembl
Outerchr7:139876100..139877000hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1122175
Supporting Variants
SamplesKWS2
Known GenesKDM7A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969617
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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